The Founder Mutation MSH2*1906G→C Is an Important Cause of...

The American Journal of Human Genetics 2002 Vol. 71; Iss. 6

The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population

W.D. Foulkes, I. Thiffault, S.B. Gruber, M. Horwitz, N. Hamel, C. Lee, J. Shia, A. Markowitz, A. Figer, E. Friedman, D. Farber, C. M.T. Greenwood, J.D. Bonner, K. Nafa, T. Walsh, V. Marcus, L. Tomsho,
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Volume:
71
Year:
2002
Language:
english
DOI:
10.1086/345075
File:
PDF, 1.10 MB
english, 2002
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